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Structure of 4683-51-6
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This bench-stable diketone features a rigid cyclopentane core with two methyl groups enhancing steric protection and solubility. The 1,3-dione system enables facile enolization and participation in aldol condensations, Michael additions, and transition-metal-catalyzed couplings. Ideal for constructing complex carbocyclic frameworks in synthetic organic chemistry and natural product synthesis.
4,4-Dimethylcyclopentane-1,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclopentanones and heterocyclic scaffolds. Its diketone functionality supports aldol condensations, Michael additions, and enolate-mediated transformations with high regiocontrol. The geminal dimethyl groups enhance steric shielding and bench stability, facilitating purification and scalability in medicinal chemistry campaigns.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: